Abstract
Objective
Controversies exist as to whether early treatment for Kawasaki disease might increase the need for additional intravenous immunoglobulin (IVIG) treatment and whether it could reduce cardiac complications. We conducted this study to add useful clues, which could be helpful when setting up a treatment plan.
Methods
359 patients who were newly diagnosed with Kawasaki disease at Severance Hospital were divided into two groups; patients who received IVIG treatment within 3 days (group A) and those who received IVIG treatment after 3 days (groups B and C). We compared the laboratory data, fever duration, frequency of additional IVIG treatment, and echocardiography follow-up results.
Results
IVIG was administered 1.11±0.34 (mean±SD), 1.15±0.39, and 1.17±0.42 times in groups A, B, and C, respectively; p=0.29 (A vs. B), p=0.21 (A vs. C). The incidence of cardiac complications checked within the first 2 weeks from disease onset was 3.6%, 5.2%, and 5.1% in groups A, B, and C, respectively; p=0.52 (A vs. B), p=0.55 (A vs. C), and the values checked at 2 months were 3.6%, 5.6%, and 5.7% in groups A, B, and C, respectively; p=0.43 (A vs. B), p=0.43 (A vs. C).
REFERENCES
1). Taubert KA., Rowley AH., Shulman ST. Nationwide survey of Kawasaki disease and acute rheumatic fever. J Pediatr. 1991. 119:279–82.
2). Kawasaki T. Acute febrile mucocutaneous syndrome with lymphoid involvement with specific desquamation of the fingers and toes in children. Arerugi. 1967. 16:178–222.
3). JCS Joint Working Group.Guidelines for diagnosis and management of cardiovascular sequelae in Kawasaki disease (JCS 2008)- digest version. Circ J. 2010. 74:1989–2020.
4). Newburger JW., Takahashi M., Gerber MA., Gewitz MH., Tani LY., Burns JC, et al. Diagnosis, treatment, and long-term management of Kawasaki disease: a statement for health professionals from the Committee on Rheumatic Fever, Endocarditis, and Kawasaki Disease, Council on Cardiovascular Disease in the Young, American Heart Association. Pediatrics. 2004. 114:1708–33.
5). Kato H., Sugimura T., Akagi T., Sato N., Hashino K., Maeno Y, et al. Long-term consequences of Kawasaki disease. A 10- to 21-year follow-up study of 594 patients. Circulation. 1996. 94:1379–85.
6). Capannari TE., Daniels SR., Meyer RA., Schwartz DC., Kaplan S. Sensitivity, specificity and predictive value of two-dimensional echocardiography in detecting coronary artery aneurysms in patients with Kawasaki disease. J Am Coll Cardiol. 1986. 7:355–60.
7). Scott JS., Ettedgui JA., Neches WH. Cost-effective use of echocardiography in children with Kawasaki disease. Pediatrics. 1999. 104:e57.
10). Durongpisitkul K., Gururaj VJ., Park JM., Martin CF. The prevention of coronary artery aneurysm in Kawasaki disease: a meta-analysis on the efficacy of aspirin and immunoglobulin treatment. Pediatrics. 1995. 96:1057–61.
11). Terai M., Shulman ST. Prevalence of coronary artery abnormalities in Kawasaki disease is highly dependent on gamma globulin dose but independent of salicylate dose. J Pediatr. 1997. 131:888–93.
12). Newburger JW., Takahashi M., Burns JC., Beiser AS., Chung KJ., Duffy CE, et al. The treatment of Kawasaki syndrome with intravenous gamma globulin. N Engl J Med. 1986. 315:341–7.
13). Newburger JW., Takahashi M., Beiser AS., Burns JC., Bastian J., Chung KJ, et al. A single intravenous infusion of gamma globulin as compared with four infusions in the treatment of acute Kawasaki syndrome. N Engl J Med. 1991. 324:1633–9.
15). Egami K., Muta H., Ishii M., Suda K., Sugahara Y., Iemura M, et al. Prediction of resistance to intravenous immunoglobulin treatment in patients with Kawasaki disease. J Pediatr. 2006. 149:237–40.
16). Sonobe T., Kawasaki T. Atypical Kawasaki disease. Prog Clin Biol Res. 1987. 250:367–78.
17). Barone SR., Pontrelli LR., Krilov LR. The differentiation of classic Kawasaki disease, atypical Kawasaki disease, and acute adenoviral infection: use of clinical features and a rapid direct fluorescent antigen test. Arch Pediatr Adolesc Med. 2000. 154:453–6.
18). Muta H., Ishii M., Egami K., Furui J., Sugahara Y., Akagi T, et al. Early intravenous gamma-globulin treatment for Kawasaki disease: the nationwide surveys in Japan. J Pediatr. 2004. 144:496–9.
19). Research Committee on Kawasaki diseases. Report of subcommittee on standardization of diagnostic criteria and reporting of coronary artery lesions in Kawasaki disease. Tokyo, Japan, Ministry of Health and Welfare. 1984.
20). Yanagawa H., Nakamura Y., Yashiro M., Oki I., Hirata S., Zhang T, et al. Incidence survey of Kawasaki disease in 1997 and 1998 in Japan. Pediatrics. 2001. 107:E33.
22). Xu C., Poirier B., Duong Van Huyen JP., Lucchiari N., Michel O., Chevalier J, et al. Modulation of endothelial cell function by normal polyspecific human intravenous immunoglobulins: a possible mechanism of action in vascular diseases. Am J Pathol. 1998. 153:1257–66.
23). Kaneka K., Savage CO., Pottinger BE., Shah V., Pearson JD., Dillon MJ. The mechanism of efficacy of intravenous immunoglobulin in Kawasaki disease. Pediatr Infect Dis J. 1994. 13:1022–3.
24). Kim T., Choi W., Woo C., Choi B., Lee J., Lee K, et al. Predictive risk factors for coronary artery abnormalities in Kawasaki disease. Eur J Pediatr. 2007. 166:421–5.
25). Zhang T., Yanagawa H., Oki I., Nakamura Y. Factors relating to the cardiac sequelae of Kawasaki disease one month after initial onset. Acta Paediatr. 2002. 91:517–20.
26). Tse SM., Silverman ED., McCrindle BW., Yeung RS. Early treatment with intravenous immunoglobulin in patients with Kawasaki disease. J Pediatr. 2002. 140:450–5.
27). Mitani Y., Sawada H., Hayakawa H., Aoki K., Ohashi H., Matsumura M, et al. Elevated levels of high-sensitivity C-reactive protein and serum amyloid-A late after Kawasaki disease: association between inflammation and late coronary sequelae in Kawasaki disease. Circulation. 2005. 111:38–43.
28). Lu CP., Lee WJ., Ho MM., Hwang KC. Risk factors of coronary arterial aneurysm in Kawasaki disease. Zhonghua Min Guo Xiao Er Ke Yu Xue Hui Za Zhi. 1993. 34:173–80.